Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D PATERSON

Showing results (431-440 of 540) with videos related to

Pageof 54
Sort By:
Journal of Neurodevelopmental Disorders|June 13, 2018
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigreesMarc Woodbury-Smith, Andrew D Paterson, Irene O'Connor, et al.
Journal of Medical Genetics|October 9, 2014
OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epitheliumAjoy Vincent, Nicole Forster, Jason T Maynes, et al.
Rheumatology (Oxford, England)|January 18, 2023
Genetics of osteonecrosis in children and adults with systemic lupus erythematosusDeclan Webber, Jingjing Cao, Daniela Dominguez, et al.
Diabetology & Metabolic Syndrome|June 3, 2017
Skin autofluorescence, a non-invasive biomarker for advanced glycation end products, is associated with the metabolic syndrome and its individual componentsRobert P van Waateringe, Sandra N Slagter, Andre P van Beek, et al.
The Journal of Clinical Endocrinology and Metabolism|October 21, 2011
Genome-wide scan for loci of adolescent obesity and their relationship with blood pressureMelkaye G Melka, Manon Bernard, Amel Mahboubi, et al.
Diabetes Care|March 6, 2019
Risk Factors for Kidney Disease in Type 1 DiabetesBruce A Perkins, Ionut Bebu, Ian H de Boer, et al.
Journal of the American Society of Nephrology : JASN|October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKDYork Pei, James Obaji, Annie Dupuis, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 5, 2017
X-Linked Glomerulopathy Due to COL4A5 Founder VariantMoumita Barua, Rohan John, Lorenzo Stella, et al.
American Journal of Human Genetics|January 8, 2013
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2Pierre Moffatt, Mouna Ben Amor, Francis H Glorieux, et al.
Metabolic Bone Disease & Related Research|January 1, 1981
Biochemical markers of bone turnover in Paget's diseaseR G Russell, D J Beard, E C Cameron, et al.
Pageof 54

Showing results (431-440 of 540) with videos related to

Sort By:
Pageof 54
Journal of Neurodevelopmental Disorders|June 13, 2018
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigreesMarc Woodbury-Smith, Andrew D Paterson, Irene O'Connor, et al.
Journal of Medical Genetics|October 9, 2014
OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epitheliumAjoy Vincent, Nicole Forster, Jason T Maynes, et al.
Rheumatology (Oxford, England)|January 18, 2023
Genetics of osteonecrosis in children and adults with systemic lupus erythematosusDeclan Webber, Jingjing Cao, Daniela Dominguez, et al.
Diabetology & Metabolic Syndrome|June 3, 2017
Skin autofluorescence, a non-invasive biomarker for advanced glycation end products, is associated with the metabolic syndrome and its individual componentsRobert P van Waateringe, Sandra N Slagter, Andre P van Beek, et al.
The Journal of Clinical Endocrinology and Metabolism|October 21, 2011
Genome-wide scan for loci of adolescent obesity and their relationship with blood pressureMelkaye G Melka, Manon Bernard, Amel Mahboubi, et al.
Diabetes Care|March 6, 2019
Risk Factors for Kidney Disease in Type 1 DiabetesBruce A Perkins, Ionut Bebu, Ian H de Boer, et al.
Journal of the American Society of Nephrology : JASN|October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKDYork Pei, James Obaji, Annie Dupuis, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 5, 2017
X-Linked Glomerulopathy Due to COL4A5 Founder VariantMoumita Barua, Rohan John, Lorenzo Stella, et al.
American Journal of Human Genetics|January 8, 2013
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2Pierre Moffatt, Mouna Ben Amor, Francis H Glorieux, et al.
Metabolic Bone Disease & Related Research|January 1, 1981
Biochemical markers of bone turnover in Paget's diseaseR G Russell, D J Beard, E C Cameron, et al.
Pageof 54